P295: Expanding the prenatal phenotype of a rare syndrome due to variants in DPH1

• Emily Dunn,
• Carly Smith,
• Catrina Loucks,
• A. Micheil Innes,
• Dena Matalon

Affiliations

Emily Dunn

Department of Pediatrics, Stanford University

Carly Smith

Fetal and Pregnancy Health Program, Stanford Medicine Children’s Health

Catrina Loucks

Division of Translational Therapeutics, Department of Pediatrics, University of British Columbia

A. Micheil Innes

Department of Medical Genetics, Cumming School of Medicine, University of Calgary

Dena Matalon

Department of Pediatrics, Stanford University